HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl iodide → HCID 131722092, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 131722093 | HCID 131722093 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 131722092 | HCID 131722092 | 175.4% |
Reaction Steps
Prepared according to the method described in Example 6(d) above from (R)-N5 -(Cbz)-N2 -(diphenylacetyl)-(R)-N-[1-(4-benzyloxyphenyl)ethyl]-ornithine amide (1.0 g; 1.49 mmol; from step (c) above), trimethylsilyliodide (0.33 g; 1.64 mmol) and CH3CN (35 mL) at 0° C., 2 hours reaction time. The resultant heterogeneous solution was submitted to aqueous work up and chromatographed on silica eluting with CH2Cl2 :MeOH:conc. NH4OH (88.5:10:1.5) to afford the sub-title compound as a solid (0.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06127414 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-bcef20769bd948fcbce8f589bc63b388 |
| Source note | uspto-grants-2000_10 |